|
rs6025
|
|
|
0.740 |
GeneticVariation |
BEFREE |
A total of nine gene variants/polymorphisms - F5 (Leiden - R5 06Q, rs6025), F2 (20210G > A, rs1799963), F13A1 (V34L, rs5985), MTHFR (677C > T - A222V, rs1801133), MTHFR (1298A > C - E429A, rs1801131), FGB (-455G > A -c.-463G > A; rs1800790), SERPINE1 (PAI14G/5G - rs1799889), ACE (ACE I/D, rs1799752), ITGB3 (GPIIIa L33P, rs5918) and the APOE E2/E3/E4 alleles (rs7412, rs429358) - were genotyped in 200 newly diagnosed ischemic stroke (IS) patients, 165 patients with ischemic coronary heart disease (CHD) and 159 controls with no cerebroor cardiovascular disease (non-CVD).
|
27629735 |
2016 |
|
rs6025
|
|
T |
0.740 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
|
26908601 |
2016 |
|
rs6025
|
|
|
0.740 |
GeneticVariation |
BEFREE |
There was no association of rs6025 with IS in general, or with any subtype.
|
25897999 |
2015 |
|
rs6025
|
|
|
0.740 |
GeneticVariation |
BEFREE |
Activated protein C resistance in ischemic stroke not due to factor V arginine506-->glutamine mutation.
|
8685921 |
1996 |
|
rs6025
|
|
|
0.740 |
GeneticVariation |
BEFREE |
The common factor V Arg 506 Gln mutation predisposing to venous thrombosis is not a significant genetic risk factor for ischemic stroke in the elderly.
|
8553401 |
1996 |
|
rs2200733
|
|
T |
0.730 |
GeneticVariation |
GWASCAT |
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
|
26708676 |
2016 |
|
rs2200733
|
|
|
0.730 |
GeneticVariation |
BEFREE |
Our results show that the SNP rs2200733</span> and r</span>s6843082 have no significant associations with IS in additive, dominant, recessive, and allelic models (all p > 0.050).
|
25711478 |
2015 |
|
rs2200733
|
|
|
0.730 |
GeneticVariation |
BEFREE |
No significant association was found between rs2200733 and ischemic stroke.
|
19707791 |
2009 |
|
rs2200733
|
|
|
0.730 |
GeneticVariation |
BEFREE |
We discovered that variants previously shown to associate with atrial fibrillation (AF), rs2200733 and rs10033464, significantly associated with IS, with the strongest risk for CES.
|
18991354 |
2008 |
|
rs10744777
|
|
|
0.720 |
GeneticVariation |
BEFREE |
The genotype of rs10744777 (CT/TT) was associated with risk of ischemic stroke in males (OR = 1.99, 95% CI = 1.15-3.42, P = 0.013).
|
30077765 |
2018 |
|
rs505922
|
|
|
0.720 |
GeneticVariation |
BEFREE |
We found that rs579459 and rs505922 within ABO gene and their interaction were both associated with increased IS risk in Chinese population.
|
28984382 |
2018 |
|
rs529565
|
|
|
0.720 |
GeneticVariation |
BEFREE |
We did not find any relation of rs651007 and rs529565 with IS risk in both additive and dominant models.
|
28984382 |
2018 |
|
rs505922
|
|
C |
0.720 |
GeneticVariation |
GWASCAT |
Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke.
|
28495826 |
2017 |
|
rs10744777
|
|
T |
0.720 |
GeneticVariation |
GWASCAT |
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
|
26708676 |
2016 |
|
rs1799963
|
|
|
0.720 |
GeneticVariation |
BEFREE |
A total of nine gene variants/polymorphisms - F5 (Leiden - R5 06Q, rs6025), F2 (20210G > A, rs1799963), F13A1 (V34L, rs5985), MTHFR (677C > T - A222V, rs1801133), MTHFR (1298A > C - E429A, rs1801131), FGB (-455G > A -c.-463G > A; rs1800790), SERPINE1 (PAI14G/5G - rs1799889), ACE (ACE I/D, rs1799752), ITGB3 (GPIIIa L33P, rs5918) and the APOE E2/E3/E4 alleles (rs7412, rs429358) - were genotyped in 200 newly diagnosed ischemic stroke (IS) patients, 165 patients with ischemic coronary heart disease (CHD) and 159 controls with no cerebroor cardiovascular disease (non-CVD).
|
27629735 |
2016 |
|
rs1799963
|
|
A |
0.720 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
|
26908601 |
2016 |
|
rs529565
|
|
|
0.720 |
GeneticVariation |
BEFREE |
We selected four single nucleotide polymorphisms (rs579459, rs651007, rs514659 and rs529565) of the ABO gene and performed genotyping assays to assess the association with ischemic stroke and its subtypes.
|
27542834 |
2016 |
|
rs529565
|
|
C |
0.720 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
|
26908601 |
2016 |
|
rs1799963
|
|
|
0.720 |
GeneticVariation |
BEFREE |
We evaluated the differences in the distribution of rs6025 and rs1799963 polymorphisms according to IS subtypes and their interaction with smoking.
|
25897999 |
2015 |
|
rs10744777
|
|
|
0.720 |
GeneticVariation |
BEFREE |
In an overall analysis of 17,970 cases of ischemic stroke and 70,764 controls, we identified a novel association on chromosome 12q24 (rs10744777, odds ratio [OR] 1.10 [1.07-1.13], p = 7.12 × 10(-11)) with ischemic stroke.
|
25031287 |
2014 |
|
rs505922
|
|
|
0.720 |
GeneticVariation |
BEFREE |
SNP rs505922 was nominally associated with ischemic stroke (odds ratio = 0.94, 95% confidence interval = 0.88-0.99, p = 0.023).
|
23381943 |
2013 |
|
rs2107595
|
|
|
0.710 |
GeneticVariation |
GWASCAT |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
29531354 |
2018 |
|
rs11196288
|
|
|
0.710 |
GeneticVariation |
BEFREE |
The results indicated that the role of rs11196288 polymorphism in ischemic stroke susceptibility in Chinese Han population may be different from that in European.
|
28501930 |
2017 |
|
rs11196288
|
|
G |
0.710 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
|
26732560 |
2016 |
|
rs2107595
|
|
A |
0.710 |
GeneticVariation |
GWASCAT |
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
|
26708676 |
2016 |